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Toplam kayıt 21, listelenen: 1-10
The IL-33 gene is related to increased susceptibility to systemic sclerosis
(Springer Heidelberg, 2016)
Systemic sclerosis (SSc) is a chronic inflammatory disease characterized by widespread fibrosis of the skin and several visceral organs. The pro-fibrotic potential of interleukin (IL)-33 has been demonstrated by in both ...
The relationship between attention deficit hyperactivity disorder and reelin gene polymorphicms in Turkish population
(Taylor & Francis Ltd, 2018)
PURPOSE: Although attention deficit hyperactivity disorder (ADHD) is one of the most frequently seen psychiatric disorders in childhood, its etiology and pathophysiology are not fully elucidated. The aim of the present ...
ENHO gene expression and serum adropin level in rheumatoid arthritis and systemic lupus erythematosus
(Wroclaw Medical Univ, 2018)
Background. Adropin, a secreted protein, is encoded by the energy homeostasis-associated gene (ENHO). It is expressed by a variety of tissues and cells. It has been implicated in several physiological and pathological ...
Serum IL-33 level and IL-33 gene polymorphisms in Behcet's disease
(Springer Heidelberg, 2015)
Beh double dagger et's disease (BD) is a chronic inflammatory disease. Increased productions of cytokines including interleukin (IL)-1 beta and IL-18 are documented, and IL-1 alpha and beta gene polymorphisms are associated ...
Chromosomal Translocation t (10; 19) (q11.2; q13.4) in an Infertile Male
(Aves, 2014)
Chromosomal rearrangements are usually associated with male factor infertility. We report here a 34-year-old man suffering from primary infertility for 15 years. The cytogenetic analysis and investigation of Y-chromosome ...
Differential Expression of MicroRNAs in Chronic Obstructive Pulmonary Disease
(Wroclaw Medical Univ, 2016)
Background. This study aimed to investigate the associations of miRNA with COPD patients. Objectives. Chronic obstructive pulmonary disease (COPD) is characterized by progressive and largely irreversible airflow limitation. ...
Methylation of cation-chloride cotransporters NKCC1 and KCC2 in patients with juvenile myoclonic epilepsy
(Springer-Verlag Italia Srl, 2019)
The etiology of juvenile myoclonic epilepsy (JME) is still unknown and the process of elaboration of multiple genetic mechanisms is ongoing. The aim of this study was to investigate the potential role of NKCC1 (SCL12A2) ...
Sirtuin gene polymorphisms are associated with chronic obstructive pulmonary disease in patients in Mugla province
(Termedia Publishing House Ltd, 2014)
Introduction: Chronic obstructive pulmonary disease (COPD) is an irreversible progressive chronic inflammatory disease that causes shortness of breath in consequence of a decrease in pulmonary functions. The pulmonary ...
Epidemiology and Carciongenesis of Lung Cancer Part B: Lung Cancer Cancerogenesis
(Bentham Science Publ, 2013)
Lung cancer is one of the most common cancers and is the leading cause of cancer mortality worldwide. The development of lung cancer is a multifactorial process that involves a series of genetic and epigenetic changes. ...
The effects of novokinin, an AT2 agonist, on blood pressure, vascular responses, and levels of ADMA, NADPH oxidase, and Rho kinase in hypertension induced by NOS inhibition and salt
(Tubitak Scientific & Technical Research Council Turkey, 2016)
Background/aim: The effects of AT 2 receptor agonist novokinin on blood pressure, eNOS, NADPH oxidase, protein arginine methyltransferases (PRMTs), and Rho kinase in hypertension were investigated. Furthermore, in isolated ...